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US3057875A - Substituted 2-methylene-4, 5-dicyano-1, 3-dithiolen compounds - Google Patents

Substituted 2-methylene-4, 5-dicyano-1, 3-dithiolen compounds Download PDF

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US3057875A
US3057875A US24234A US2423460A US3057875A US 3057875 A US3057875 A US 3057875A US 24234 A US24234 A US 24234A US 2423460 A US2423460 A US 2423460A US 3057875 A US3057875 A US 3057875A
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dicyano
dithiolene
methylene
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/45—Heterocyclic compounds having sulfur in the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
    • C07D339/02—Five-membered rings
    • C07D339/06—Five-membered rings having the hetero atoms in positions 1 and 3, e.g. cyclic dithiocarbonates

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  • a preferred class of compounds within Formula 2 are those wherein A and B are united to the methylene carbon through a polyvalent atom of the group C, N, and S, are the same or different, and are selected from the group consisting of CN, COOR, SO R, -SO NR CONH CONHR, CONR -COR; A and B together can form a divalent radical selected from the group consisting of CO--RCO, e.g., CO(CH -CO and In this preferred class R and R are monovalent and divalent hydrocarbon groups free of non-aromatic unsaturation (i.e., in which any unsaturation is aromatic) of up to 7 carbons (i.e., 1 through 7 carbons) each.
  • the products of this invention can be prepared by reacting a 1,2-dihalo-1,Z-dicyanoethylene with a salt of a 1,1- dimercapto-2,2-disubstituted ethylene.
  • This reaction and the structural formulas of the reactants can be represented as follows:
  • Equation No. 3 (supra)
  • X in Formula A is a halogen atom, i.e., fluorine, chlorine or bromine, but preferably chlorine.
  • M in Formula B represents an alkali metal or an alkyl substituted ammonium cation. A and B in this latter formula are as defined above.
  • triethylammonium, sodium and potassium salts are typical preferred examples.
  • 1,2dihalo-1,2-dicyanoethylene and the 1,1-dimercapto-2,Z-disubstituted ethylene salts are simply contacted in a conventional reaction vessel. Elevated or reduced temperatures are not critical factors in the process, but the reaction seems to produce the best yields at temperatures from about 10 to 30 C. However, temperatures as low as about C. or as high as about C., or even higher, can be used.
  • the reaction time can be varied between wide limits. In a batch process it is generally between about 10 minutes and 24 hours. The time can be varied inversely with both the temperature and the reactivity of the reactants.
  • Mole ratios of reactants are also not critical, but in a preferred process the two reactants are used in a 1:1 mole ratio as the stoichiometry of Equation 3 above suggests. However, an excess of either reactant can be used when and if desired.
  • an inert pref erably organic liquid reaction medium i.e., in a medium which is inert to reactants and products under the particular reaction conditions chosen.
  • Suitable media include such commonly available materials as tetrahydrofuran, ethanol, methanol, diethyl ether, 1,2-dimethoxyethane, dioxane, acetonitrile, dimethyl sulfoxide, ethyl acetate, benzene, cyclohexane, and dimethylformamide.
  • Other suitable reaction media will be readily apparent to those skilled in the art.
  • the desired substituted 2methylene-4,5-dicyano- 1,3-dithiolene is separated from the reaction mixture by conventional means and similarly purified to the extent desired.
  • the compounds thus obtained are in general yellow, crystalline, high-melting substances with strong absorption in the ultraviolet region above 300 mg.
  • 1,2-dihalo-1,2-dicyanoethylenes of Formula 3 (A) useful in the processes of preparing the compounds of this invention can be prepared by any conventional means.
  • 1,2-dichloro-1,Z-dicyanoethylene can be prepared as described in US. Patent 2,443,494, and it can be used in either the cis-form (dichloromaleonitrile) or in the transform (dichlorofumaronitrile) or as a mixture of both cisand trans-form.
  • salts of 1,1-dimercapto-2,2-disubstituted ethylenes can be prepared by any conventional means known to the art.
  • Especially practical salts are the disodium and dipotassium salts which can readily be prepared by slightly varying the methods described in US. Patents 2,493,071 and 2,533,233 which involve the reaction of carbon disulfide and the appropriate active methylene compound in alcoholic base. This reaction can be represented as follows:
  • the infrared spectrum shows absorption at 4.48 (conjugated CN), 6.48,, 6.67 and 7.73;.
  • the infrared spectrum shows absorption at 4.5,u, 6.50 2, 6.85 and 8.45
  • Dithiolene Example I is repeated using ethyl cyanoacetate instead of malononitrile to give dipotassium 1,1-dimercapto-2- cyano-2-carboethoxyethylene which is a light yellow solid having no melting point below 250 C.
  • the ultraviolet spectrum shows AOHZCIQ 347 me 10:77
  • Dipotassium 1,1-dirnercapto-Z-cyano-Z-carboxamidoethylene is treated with dichlorofumaronitrile according to the procedure of Example II to give 95% of the theoretical yield of a yellow solid, 2-(cyanocarboxarnidomethylene)-4,5-dicyano-1,3-dithiolene, melting at 288- 295 C. (decomp.).
  • Three crystallizations of this product from a mixture of acetone and tetrahydrofuran gave a a 73% yield of fine yellow needles, M.P. 298-300 C. (decomp.).
  • the infrared spectrum shows absorption at 2.88 1. and 2.98 1.
  • NH 4.49 1 conjuggated CN
  • dimercapto-2-cyano-2-p-toluenesulfonylethylene in 68% of the theoretical yield, a yellow solid, which did not melt but decomposed above about 250 C.
  • dithiolene of Example V as the light screening agent.
  • These tests show that small amounts, e.g., 0.1 to 5%, of the substituted 2-methylene-4,5-dicyano-1,3-dithiolenes of this invention are useful for the protection of light-sensitive materials and can be used in various ways such as a shield as illustrated above, as a coating directly on the object, o as a component of the object for which light protection is required.
  • Light-sensitive materials which can be protected in this manner are illustrated by films of regenerated cellulose, cellulose acetate, polyvinyl chloride, ethylene glyco terephthalate polyester resin films, protective coatings including clear varnishes and both dyed and undyed natural and synthetic fibers and fabrics.
  • a and B taken singly, are selected from the class consisting of CN, --COOR, SO R, -SO NR CONH -CONHR, -CONR and -COR, R being hydrocarbon free of non-aromatic unsaturation of up to seven carbon atoms; and A and B, taken together, are a divalent radical selected from the class consisting of OTHER REFERENCES Bahr et al.: Chemischetechnik, vol. 8, pages 597-8 (1956).

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Description

3357525 Patented @ct. a, 1952 I use 3,057,875 SUBSTITUTED 2-METHYLENE-4,5-DICYANO- LS-DITHEQLEN COMPOUNDS Morton Brown, Wilmington, Del, assiguor to E. I. du Pont de Nemours and Company, Wilmington, Del, a corporation of Delaware N Drawing. Filed Apr. 25, 1960, Ser. No. 24,234 Claims. (Cl. 260327) This invention relates to new and useful derivatives of 1,3-dithiolene 1,3-dithiolene has the formula oH=oH A Q B wherein A and B, when taken individually, constitute monovalent groups which are attached to the methylene carbon shown in Formula 2 through a polyvalent atom, this atom being part of the monovalent group, which in turn is attached to another atom by a multiple bond; and wherein A and B can be united to form a divalent group, each terminal atom of which is united to the methylene carbon through a polyvalent atom, at least one of which in turn is attached to another atom by a multiple bond. A preferred class of compounds within Formula 2 are those wherein A and B are united to the methylene carbon through a polyvalent atom of the group C, N, and S, are the same or different, and are selected from the group consisting of CN, COOR, SO R, -SO NR CONH CONHR, CONR -COR; A and B together can form a divalent radical selected from the group consisting of CO--RCO, e.g., CO(CH -CO and In this preferred class R and R are monovalent and divalent hydrocarbon groups free of non-aromatic unsaturation (i.e., in which any unsaturation is aromatic) of up to 7 carbons (i.e., 1 through 7 carbons) each.
The products of this invention can be prepared by reacting a 1,2-dihalo-1,Z-dicyanoethylene with a salt of a 1,1- dimercapto-2,2-disubstituted ethylene. This reaction and the structural formulas of the reactants can be represented as follows:
In Equation No. 3 (supra) X in Formula A is a halogen atom, i.e., fluorine, chlorine or bromine, but preferably chlorine. Similarly, in Equation 3 M in Formula B represents an alkali metal or an alkyl substituted ammonium cation. A and B in this latter formula are as defined above.
Of the cationic salts of l,1-dimercapto-2,2-disubstituted ethylenes represented by Formula B, triethylammonium, sodium and potassium salts are typical preferred examples.
In general, the 1,2dihalo-1,2-dicyanoethylene and the 1,1-dimercapto-2,Z-disubstituted ethylene salts are simply contacted in a conventional reaction vessel. Elevated or reduced temperatures are not critical factors in the process, but the reaction seems to produce the best yields at temperatures from about 10 to 30 C. However, temperatures as low as about C. or as high as about C., or even higher, can be used.
The reaction time can be varied between wide limits. In a batch process it is generally between about 10 minutes and 24 hours. The time can be varied inversely with both the temperature and the reactivity of the reactants.
For convenience, the processes are conducted at atmospheric pressures, but pressures above or below atmospheric can be used.
Mole ratios of reactants are also not critical, but in a preferred process the two reactants are used in a 1:1 mole ratio as the stoichiometry of Equation 3 above suggests. However, an excess of either reactant can be used when and if desired.
In preparing the products of this invention an excess of free alkali or alkaline reagent should be avoided. This precaution is especially important in those instances where salts of 1,l-dimercapto-2,2disubstituted ethylenes are used without isolation from the reaction medium in which they are made.
It is preferred to conduct the processes in an inert pref erably organic liquid reaction medium, i.e., in a medium which is inert to reactants and products under the particular reaction conditions chosen. Suitable media include such commonly available materials as tetrahydrofuran, ethanol, methanol, diethyl ether, 1,2-dimethoxyethane, dioxane, acetonitrile, dimethyl sulfoxide, ethyl acetate, benzene, cyclohexane, and dimethylformamide. Other suitable reaction media will be readily apparent to those skilled in the art.
After the reaction between reactants is complete, or nearly so, the desired substituted 2methylene-4,5-dicyano- 1,3-dithiolene is separated from the reaction mixture by conventional means and similarly purified to the extent desired.
The compounds thus obtained are in general yellow, crystalline, high-melting substances with strong absorption in the ultraviolet region above 300 mg.
The 1,2-dihalo-1,2-dicyanoethylenes of Formula 3 (A) useful in the processes of preparing the compounds of this invention can be prepared by any conventional means. For example, 1,2-dichloro-1,Z-dicyanoethylene can be prepared as described in US. Patent 2,443,494, and it can be used in either the cis-form (dichloromaleonitrile) or in the transform (dichlorofumaronitrile) or as a mixture of both cisand trans-form.
Similarly, salts of 1,1-dimercapto-2,2-disubstituted ethylenes can be prepared by any conventional means known to the art. Especially practical salts are the disodium and dipotassium salts which can readily be prepared by slightly varying the methods described in US. Patents 2,493,071 and 2,533,233 which involve the reaction of carbon disulfide and the appropriate active methylene compound in alcoholic base. This reaction can be represented as follows:
( KS A Dipomssium 1 ,1 -Dimercapto-2,Z-Dicyanoethylene Dipotassium 1, 1-dirnercapto-2,2-dicyanoethylene,
(KS) C=C(CN) is produced as illustrated in general Equation 4 by the following procedure:
In a one-liter, three-necked flask fitted with a stirrer, thermometer, and dropping funnel is placed a solution of 60 g. of potassium hydroxide in 650 ml. of denatured ethyl alcohol. The solution is cooled to in an icesalt bath and 35.4 g. (0.536 mole) of freshly distilled malononitrile is added all in one portion followed by the dropwise addition of 41 g. (0.54 mole) of carbon disulfide at 010 C. Toward the end of the addition, a canary-yellow salt begins to precipitate. After stirring for one hour more at 05 C., the solid is collected on a filter and Washed with 50 ml. of cold ethanol. After drying to constant weight at 0.1 mm. and 80 C., there is obtained 109 g. (94% of the theoretical yield) of a yellow, water-soluble salt which does not melt below 250 C. This product is dipotassium 1,1-dimercapto- 2,2-dicyanoethylene and is of sufficient purity for subsequent reactions.
Analysis-Calcd. for C N S K Found: C, 21.76; S, 29.23.
The ultraviolet spectrum had W 343 m (k=48) max.
and a shoulder at 215 mu (k=28). The infrared had absorption at 4.5; (conjugated CN) and 6.30 (C=C).
EXAMPLE II 2-Dicyanomethylene-4,5-Dicyano-1,3-Dithi0lene 2-Dicyanomethylene-4,S-dicyano-1,3-dithiolene,
N C-C- S C N is produced as illustrated in general Equation 3 by the following procedure. Ninety-four grams of dipotassium 1,l-dimercapto-2,2-dicyanoethylene (0.43 mole) prepared as described in Example I is suspended in 500 ml. of dry tetrahydrofuran in a flask protected with calcium chloride drying tubes and cooled to 0 C. in an ice-salt bath. Dichlorofumaronitrile (49.5 g., 0.336 mole) is added in one portion and the temperature rises to 20 C. in a few minutes. The reddish-orange solution becomes black on stirring overnight. After filtration, the
filtrate is evaporated under reduced pressure leaving a gummy black residue. The residue is extracted with four ZOO-ml. portions of boiling toluene. The combined extracts are treated with decolorizing carbon and concentrated to ml. Cooling produces 36 g. (50%) of bright yellow crystals melting at 161-l70 C. with decomposition. Three recrystallizations from toluene afford 2 dicyanomethylene 4,5 dicyano 1,3-dithiolene melting at 203-206 C. with slight decomposition.
Analysis.Calcd. for C N S C, 44.43; N, 25.93; S, 29.64. Found: C, 44.68; N, 2570'; S, 30.00.
The infrared spectrum shows absorption at 4.48 (conjugated CN), 6.48,, 6.67 and 7.73;. The ultra-violet spectrum show r335 237 m (k=43.5) 283 m (k=20.9), 355 m (k=89.0), and 367 my. (k=81).
EXAMPLE III To a solution of 2.50 g. (0.0115 mole) of dipotassium 1,1-dimercapto-2,2-dicyanoethylene in 50 ml. of methanol is added in one lot 1.47 g. (0.01 mole) of dichlorofumaronitrile at room temperature. After stirring for 15 minutes, the reaction mixture is poured into 300 ml. of water and the solid which precipitates is collected on a filter (1.12 g.). Recrystallization from hot toluene after treatment with decolorizing carbon yields 0.99 g. of yellow needles, M.P. 208209 C. This is shown by elementary analysis and absorption spectra to be 2-dicyanomethylene-4,5-dicyano-1,3-dithiolene.
Analysis.-Calcd. for C N S C, 44.43; S, 2964. Found: C, 43.97; S, 30.01.
The infrared spectrum shows absorption at 4.5,u, 6.50 2, 6.85 and 8.45 The ultraviolet spectrum shows xgggf 241 m (k=56) 328 m (k=64.3), 344 mp (k=73.2), and 355 m (k=71.3).
EXAMPLE IV To a mixture of 6.6 g. (0.1 mole) of malononitrile, 20.0 g. (0.2 mole) of triethylamine, and 75 ml. of methanol is added slowly 7.6 g. (0.1 mole) of carbon disulfide while the mixture is cooled in an ice bath. The mixture is stirred 15 minutes and 14.7 g. (0.1 mole) of dichloro fumaronitrile is added in small batches over 30 minutes. The mixture is stirred an additional 30 minutes and then diluted with 100 ml. of water and allowed to stand 15 minutes. Filtration gives 23 g. (wet) of black filter cake. Extraction of this residue with hot toluene and treatment with decolorizing carbon yields 8.7 g. of product, M.P. 176179 C. The infrared spectrum shows this material to be largely 2rdicyanomethylene-4,S-dicyano-1,3-dithiolene. Trituration of the above material with hot methanol yields two fractions:
(a) Methanol insoluble, weight, 3.4 g., light yellow crystals, M.P. 205208 C. whose infrared absorption spectra show it to be identical with 2-dicyanomethylene- 4,5-dicyano-1,3-dithiolene, and
(b) The methanol-soluble portion which, after crystallization from methanol, weighs 3.1 g., M.P. 192-198" C., and is shown by infrared analysis to be largely 2-dicyano' methylene-4,5-dicyano-1,3-dithiolene.
EXAMPLE V 2-(Cyanocarboezhoxymethylene)-4 ,5 -Dicyan0-1 ,3-
Dithiolene Example I is repeated using ethyl cyanoacetate instead of malononitrile to give dipotassium 1,1-dimercapto-2- cyano-2-carboethoxyethylene which is a light yellow solid having no melting point below 250 C.
Analysis.-Calcd. for C H NO S K C, 27.21; H, 1.90; N, 5.28; S, 24.10. Found: C, 27.34, 27.24; H, 1,95, 180; N, 5.37, 5.51; S, 23.88, 24.01.
The infrared spectrum shows bands at 4.5 (conjugated CN), 6.0,u. (conjugated CO C H and 6.35 =C).
2 (cyanocarboethoxymethylene) 4,5 dicyano 1,3- dithiolene is synthesized in 66% yield in a manner similar to that of Example II using the above dipotassium 1,1- dimercapto-2-cyano-2-carboethoxyethylene with dichlorofumaronitrile as the reactants and 1,2-dimethoxyethane as the reaction solvent. It is a faintly yellow crystalline solid and melts at 137139 C. after recrystallization from hexane-benzene.
Analysis.Calcd. for C I-I N S O C, 45.70; H, 1.90; N, 15.96; S, 24.35. Found: C, 45.49, 45.80; H, 1.88, 1.77; N, 16.16; S, 24.30.
The ultraviolet spectrum shows AOHZCIQ 347 me 10:77)
IIIBX.
with a shoulder at 230m (k=41.9). In the infrared region, it shows absorption at 3.35 4.5011, 5.93 6.46 6.75;, and 7.25 14.
EXAMPLE VI 2- (Cyanocarboxamidomethylene) -4,5-Dicyan- 1,3-Dithi0lene Example I is repeated using cyanoacetamide instead of malononitrile to give, after drying to constant Weight at 80 C. at 1 mm. pressure, 73% of the theoretical yield of dipotassium 1,1-dimercapto-2-cyano-2-carboxamidoethylene, a bright yellow solid which did not melt but decomposed at about 250 C.
Dipotassium 1,1-dirnercapto-Z-cyano-Z-carboxamidoethylene is treated with dichlorofumaronitrile according to the procedure of Example II to give 95% of the theoretical yield of a yellow solid, 2-(cyanocarboxarnidomethylene)-4,5-dicyano-1,3-dithiolene, melting at 288- 295 C. (decomp.). Three crystallizations of this product from a mixture of acetone and tetrahydrofuran gave a a 73% yield of fine yellow needles, M.P. 298-300 C. (decomp.).
Analysis.-Calcd. for C H ON S C, 41.02; H, 0.85;
S, 27.37; N, 23.92. Found: C, 41.37; H, 1.03; S, 27.46; 5 N, 23.40.
The infrared spectrum shows absorption at 2.88 1. and 2.98 1. (NH 4.49 1 (conjugated CN), 6.02 1 (conjugated C=O), 6.25 1 and 6.48;; (C=C). The ultraviolet spectrum shows absorption at 345 III/L (17:87.1) and a shoulder at 230 m (k=56.8).
EXAMPLE VII 2-(Cyano-p-Toluenesulfonylmethylene) -4,5- Dicyan0-1,3-Dithi0lene Example I is repeated using p-toluenesulfonylacetonitrile instead of malononitrile to give dipotassium 1,1-
dimercapto-2-cyano-2-p-toluenesulfonylethylene in 68% of the theoretical yield, a yellow solid, which did not melt but decomposed above about 250 C.
Dipotassium 1, l-dimercapto-Z-cyano-2-p-toluenesulfonylethylene is treated with dichlorofumaronitrile according to the procedure of Example II to give 75% of the theoretical yield of a bronze-colored solid, 2-(cyano-ptoluenesulfonylmethylene) 4,5 dicyano 1,3 dithiolene, M.P. 130145 C. (deco-mp). Four crystallizations of this product from chloroform-hexane gave 46% of the theoretical yield of yellow needles, M.P. 141-142 C. decomp.
Analysis.Ca1cd. for C H O N S C, 48.68; H, 2.04; N, 12.15. Found: C, 48.63; H, 2.11; N, 12.26.
The infrared spectrum shows absorption for saturated CH at 3.1 1, conjugated CN at 4.51/.L, aromatic C=C at 6.1 1, and aliphatic C=C at 6.25 1.
Using the procedure set forth in Example II and reactants in essentially 1:1 mol ratio, the 2-metl1ylene-1,3- dithiolenes in Table I can be prepared:
TABLE I [2Methylene-1,3-Pithiolenes] Example N o. Reactants Reaetants Product A NCCS A 0X(0N)=OX(0N) (MS)gO=C =0 B NCC-S B CN 01 00202115 I N0CS 00202115 VIII (N8.S)20=C =0 31 (IN OO2O2H5 N00-S 0020211 Cl 01 0O-CH3 NGOS (JO-0H3 IX (KS)zC=C C=C JN JN 002082111 NCCS COzCsHu (31 JN 0020111 NCCS COzCzH5 CN 01 CO-GeHs N0CS OO-CuHs XI (KS)2C=0 I =0 C1 C1 (IO-CH3 NOCS (IO-43H: II 3: (KS)O=0 =0 CN 01 CO-OaHo N00S 0 OC0H5 XIII 3: (N8S)2C=C 0:0
TABLE IC0ntinuer1 [2-Methylene-l,3-Pithiolenes] Continued The substituted 2-methylene-4,5-dicyano-1,3-dithiolenes one-half of a swatch of Dacron polyester fabric which of this invention are useful as ultraviolet light absorbers had been dyed with a xanthene dye (Rhodamine 3B). for the protection of light-sensitive materials from the 70 After 100 hours of exposure to the ultraviolet light of harmful rays of sunlight. the Fade-O-Meter, the unshielded portion of the swatch Thus, in accelerated (Fade-O-Meter) tests, a 1.5 mil was very badly faded but there was little or no fading thick film of cellulose acetate containing 0.5% by weight in the shielded portion of the fabric. Approximately of the 2-dicyanornethylene-4,5-dicyano-1,3-dithiolene of equivalent results were obtained in similar tests using Example II (M.P. 203-206 C.) was used as a-shield over 75 2 (cyanocarboethoxymethylene) 4,5 dicyano 1,3- 1
dithiolene of Example V as the light screening agent. These tests show that small amounts, e.g., 0.1 to 5%, of the substituted 2-methylene-4,5-dicyano-1,3-dithiolenes of this invention are useful for the protection of light-sensitive materials and can be used in various ways such as a shield as illustrated above, as a coating directly on the object, o as a component of the object for which light protection is required. Light-sensitive materials which can be protected in this manner are illustrated by films of regenerated cellulose, cellulose acetate, polyvinyl chloride, ethylene glyco terephthalate polyester resin films, protective coatings including clear varnishes and both dyed and undyed natural and synthetic fibers and fabrics.
The foregoing detailed description has been given for clearness of understanding only and no unnecessary limitations are to be understood therefrom. The invention is not limited to the exact details shown and described, for obvious modifications Will occur to those skilled in the art.
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. 2-dicyanomethylene-4,5-dicyano-1,3-dithiolene.
2. 2 (cyanocarboethoxymethylene) 4,5 dicyano 1, S-dithiolene.
3. 2 (cyanoc-arboxamidomethylene) 4,5 dicyano- 1,3-dithiolene.
4. 2 (cyano p toluenesulfonylmethylene) 4,5 dicyano-1,3-dithiolene.
5. Compounds of the formula wherein A and B, taken singly, are selected from the class consisting of CN, --COOR, SO R, -SO NR CONH -CONHR, -CONR and -COR, R being hydrocarbon free of non-aromatic unsaturation of up to seven carbon atoms; and A and B, taken together, are a divalent radical selected from the class consisting of OTHER REFERENCES Bahr et al.: Chemische Technik, vol. 8, pages 597-8 (1956).

Claims (2)

1. 2-DICYANOMETHYLENE-4,5-DICYANO-1,3-DITHIOLENE.
5. COMPOUNDS OF THE FORMULA
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US3154573A (en) * 1961-06-05 1964-10-27 Rohm & Haas Process for preparing fluorinated dinitriles
US3960921A (en) * 1974-03-15 1976-06-01 Phillips Petroleum Company Dihalodicyano alkenes
US4312991A (en) * 1979-05-10 1982-01-26 International Business Machines Corporation Dithiobenzoate 4,5-dicyano-1,3-(dithiolidene-2-yl)methylene
EP0242061A3 (en) * 1986-03-19 1988-11-02 Hokko Chemical Industry Co., Ltd New 1,3-dithiol-2-ylidene-alkylsulfonylacetates and their uses
EP0357783A4 (en) * 1988-03-09 1991-09-11 Sumitomo Electric Industries, Ltd Secondary non-linear optical material and non-linear optical element prepared therefrom

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US2493071A (en) * 1945-08-17 1950-01-03 Ilford Ltd Sulfur-containing carboxylic acid esters

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Cited By (5)

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Publication number Priority date Publication date Assignee Title
US3154573A (en) * 1961-06-05 1964-10-27 Rohm & Haas Process for preparing fluorinated dinitriles
US3960921A (en) * 1974-03-15 1976-06-01 Phillips Petroleum Company Dihalodicyano alkenes
US4312991A (en) * 1979-05-10 1982-01-26 International Business Machines Corporation Dithiobenzoate 4,5-dicyano-1,3-(dithiolidene-2-yl)methylene
EP0242061A3 (en) * 1986-03-19 1988-11-02 Hokko Chemical Industry Co., Ltd New 1,3-dithiol-2-ylidene-alkylsulfonylacetates and their uses
EP0357783A4 (en) * 1988-03-09 1991-09-11 Sumitomo Electric Industries, Ltd Secondary non-linear optical material and non-linear optical element prepared therefrom

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